Canonical Allele Identifier: CA813299217

Gene: MAST4

Linked Data

• dbSNP Id: rs1221709848
• gnomAD v3: 5-67156240-CAGA-C
• gnomAD v4: 5-67156240-CAGA-C
• MyVariant Identifiers: chr5:g.66452069_66452071del (hg19) ; chr5:g.67156241_67156243del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.67156247_67156249del , CM000667.2:g.67156247_67156249del	GRCh38
NC_000005.9:g.66452075_66452077del , CM000667.1:g.66452075_66452077del	GRCh37
NC_000005.8:g.66487831_66487833del	NCBI36
NG_034036.1:g.564900_564902del

Transcript Alleles

HGVS	Amino-acid change
ENST00000403625.7:c.3648+2667_3648+2669del MANE Select	ENSP00000385727.1:n.3648+2667_3648+2669de...
ENST00000261569.11:c.3066+2667_3066+2669del	ENSP00000261569.7:n.3066+2667_3066+2669de...
ENST00000403625.6:c.3648+2667_3648+2669del	ENSP00000385727.1:n.3648+2667_3648+2669de...
ENST00000403666.5:c.3081+2667_3081+2669del	ENSP00000384313.1:n.3081+2667_3081+2669de...
ENST00000405643.5:c.3111+2667_3111+2669del	ENSP00000384099.1:n.3111+2667_3111+2669de...
ENST00000443808.1:c.817+2667_817+2669del
NM_001164664.1:c.3648+2667_3648+2669del	NP_001158136.1:n.3648+2667_3648+2669del
NM_001290226.1:c.3030+2667_3030+2669del	NP_001277155.1:n.3030+2667_3030+2669del
NM_001290227.1:c.2865+2667_2865+2669del	NP_001277156.1:n.2865+2667_2865+2669del
NM_001297651.1:c.3066+2667_3066+2669del	NP_001284580.1:n.3066+2667_3066+2669del
NM_015183.2:c.3081+2667_3081+2669del	NP_055998.1:n.3081+2667_3081+2669del
XM_006714606.2:c.3066+2667_3066+2669del	XP_006714669.1:n.3066+2667_3066+2669del
XM_006714610.1:c.2865+2667_2865+2669del	XP_006714673.1:n.2865+2667_2865+2669del
XM_011543381.1:c.3945+2667_3945+2669del	XP_011541683.1:n.3945+2667_3945+2669del
XM_011543382.1:c.3759+2667_3759+2669del	XP_011541684.1:n.3759+2667_3759+2669del
XM_011543383.1:c.3684+2667_3684+2669del	XP_011541685.1:n.3684+2667_3684+2669del
XM_011543384.1:c.3048+2667_3048+2669del	XP_011541686.1:n.3048+2667_3048+2669del
XM_011543385.1:c.3021+2667_3021+2669del	XP_011541687.1:n.3021+2667_3021+2669del
XM_011543386.1:c.3012+2667_3012+2669del	XP_011541688.1:n.3012+2667_3012+2669del
XM_006714606.3:c.3066+2667_3066+2669del	XP_006714669.1:n.3066+2667_3066+2669del
XM_006714610.2:c.2865+2667_2865+2669del	XP_006714673.1:n.2865+2667_2865+2669del
XM_011543384.2:c.3048+2667_3048+2669del	XP_011541686.1:n.3048+2667_3048+2669del
XM_011543385.3:c.3021+2667_3021+2669del	XP_011541687.1:n.3021+2667_3021+2669del
XM_011543386.2:c.3012+2667_3012+2669del	XP_011541688.1:n.3012+2667_3012+2669del
XM_017009449.1:c.3102+2667_3102+2669del	XP_016864938.1:n.3102+2667_3102+2669del
XM_017009450.1:c.3045+2667_3045+2669del	XP_016864939.1:n.3045+2667_3045+2669del
XM_017009451.1:c.2844+2667_2844+2669del	XP_016864940.1:n.2844+2667_2844+2669del
XM_017009452.1:c.2604+2667_2604+2669del	XP_016864941.1:n.2604+2667_2604+2669del
XM_017009453.1:c.2604+2667_2604+2669del	XP_016864942.1:n.2604+2667_2604+2669del
XM_024446044.1:c.3864+2667_3864+2669del	XP_024301812.1:n.3864+2667_3864+2669del
NM_001164664.2:c.3648+2667_3648+2669del MANE Select	NP_001158136.1:n.3648+2667_3648+2669del
NM_001290226.2:c.3030+2667_3030+2669del	NP_001277155.1:n.3030+2667_3030+2669del
NM_001290227.2:c.2865+2667_2865+2669del	NP_001277156.1:n.2865+2667_2865+2669del
NM_001297651.2:c.3066+2667_3066+2669del	NP_001284580.1:n.3066+2667_3066+2669del
NM_015183.3:c.3081+2667_3081+2669del	NP_055998.1:n.3081+2667_3081+2669del
NM_001393524.1:c.3657+2667_3657+2669del	NP_001380453.1:n.3657+2667_3657+2669del
NM_001393525.1:c.3447+2667_3447+2669del	NP_001380454.1:n.3447+2667_3447+2669del
NM_001393526.1:c.2880+2667_2880+2669del	NP_001380455.1:n.2880+2667_2880+2669del
NM_001393527.1:c.2865+2667_2865+2669del	NP_001380456.1:n.2865+2667_2865+2669del
NM_001393528.1:c.2844+2667_2844+2669del	NP_001380457.1:n.2844+2667_2844+2669del