Canonical Allele Identifier: CA361652281

Gene: SPINK5

Linked Data

• MyVariant Identifiers: chr5:g.147510953G>T (hg19) ; chr5:g.148131390G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148131390G>T , CM000667.2:g.148131390G>T	GRCh38
NC_000005.9:g.147510953G>T , CM000667.1:g.147510953G>T	GRCh37
NC_000005.8:g.147491146G>T	NCBI36
NG_009633.1:g.72419G>T , LRG_110:g.72419G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256084.8:c.3095+1G>T MANE Select	ENSP00000256084.7:n.3095+1G>T
ENST00000256084.7:c.3095+1G>T	ENSP00000256084.7:n.3095+1G>T
ENST00000359874.7:c.3185+1G>T	ENSP00000352936.3:n.3185+1G>T
NM_001127698.1:c.3185+1G>T	NP_001121170.1:n.3185+1G>T
NM_006846.3:c.3095+1G>T , LRG_110t1:c.3095+1G>T	NP_006837.2:n.3095+1G>T
XM_011537550.1:c.3128+1G>T	XP_011535852.1:n.3128+1G>T
XM_011537551.1:c.3101+1G>T	XP_011535853.1:n.3101+1G>T
XM_011537551.2:c.3101+1G>T	XP_011535853.1:n.3101+1G>T
NM_001127698.2:c.3185+1G>T	NP_001121170.1:n.3185+1G>T
NM_006846.4:c.3095+1G>T MANE Select	NP_006837.2:n.3095+1G>T