Canonical Allele Identifier: CA3581364

Gene: F12 GRK6 SLC34A1

Linked Data

• dbSNP Id: rs771165528
• ExAC: 5:176831368 C / A
• gnomAD v2: 5-176831368-C-A
• gnomAD v3: 5-177404367-C-A
• gnomAD v4: 5-177404367-C-A
• MyVariant Identifiers: chr5:g.176831368C>A (hg19) ; chr5:g.177404367C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177404367C>A , CM000667.2:g.177404367C>A	GRCh38
NC_000005.9:g.176831368C>A , CM000667.1:g.176831368C>A	GRCh37
NC_000005.8:g.176763974C>A	NCBI36
NG_007568.1:g.10210G>T , LRG_145:g.10210G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696192.1:c.*513G>T (F12)	ENSP00000512476.1:n.*513G>T
ENST00000696193.1:c.*1217G>T (F12)	ENSP00000512477.1:n.*1217G>T
ENST00000696194.1:c.*437G>T (F12)	ENSP00000512478.1:n.*437G>T
ENST00000696195.1:n.3650G>T (F12)
ENST00000696200.1:n.950G>T (F12)
ENST00000696201.1:c.847G>T (F12)	ENSP00000512482.1:p.Asp283Tyr
ENST00000253496.4:c.847G>T (F12) MANE Select	ENSP00000253496.3:p.Asp283Tyr
ENST00000253496.3:c.847G>T (F12)	ENSP00000253496.3:p.Asp283Tyr
ENST00000502598.5:c.-45+841C>A (GRK6)	ENSP00000422873.1:n.-45+841C>A
ENST00000502854.5:n.106G>T (F12)
ENST00000503736.1:n.219G>T (F12)
ENST00000510358.5:n.106G>T (F12)
NM_000505.3:c.847G>T , LRG_145t1:c.847G>T (F12)	NP_000496.2:p.Asp283Tyr
XM_011534461.1:c.847G>T (F12)	XP_011532763.1:p.Asp283Tyr
XM_011534462.1:c.511G>T (F12)	XP_011532764.1:p.Asp171Tyr
XM_011534462.2:c.511G>T (F12)	XP_011532764.1:p.Asp171Tyr
XM_017009773.2:c.1416+7293C>A (SLC34A1)	XP_016865262.1:n.1416+7293C>A
NM_000505.4:c.847G>T (F12) MANE Select	NP_000496.2:p.Asp283Tyr