Canonical Allele Identifier: CA361652011

Gene: SPINK5

Linked Data

• MyVariant Identifiers: chr5:g.147510855C>A (hg19) ; chr5:g.148131292C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148131292C>A , CM000667.2:g.148131292C>A	GRCh38
NC_000005.9:g.147510855C>A , CM000667.1:g.147510855C>A	GRCh37
NC_000005.8:g.147491048C>A	NCBI36
NG_009633.1:g.72321C>A , LRG_110:g.72321C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256084.8:c.2998C>A MANE Select	ENSP00000256084.7:p.Pro1000Thr
ENST00000256084.7:c.2998C>A	ENSP00000256084.7:p.Pro1000Thr
ENST00000359874.7:c.3088C>A	ENSP00000352936.3:p.Pro1030Thr
NM_001127698.1:c.3088C>A	NP_001121170.1:p.Pro1030Thr
NM_006846.3:c.2998C>A , LRG_110t1:c.2998C>A	NP_006837.2:p.Pro1000Thr
XM_011537550.1:c.3031C>A	XP_011535852.1:p.Pro1011Thr
XM_011537551.1:c.3004C>A	XP_011535853.1:p.Pro1002Thr
XM_011537551.2:c.3004C>A	XP_011535853.1:p.Pro1002Thr
NM_001127698.2:c.3088C>A	NP_001121170.1:p.Pro1030Thr
NM_006846.4:c.2998C>A MANE Select	NP_006837.2:p.Pro1000Thr