Canonical Allele Identifier: CA399389262
Gene: KRT12 HGNC NCBI

Linked Data

dbSNP Id: rs2143270838

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867009C>A , CM000679.2:g.40867009C>A GRCh38
NC_000017.10:g.39023261C>A , CM000679.1:g.39023261C>A GRCh37
NC_000017.9:g.36276787C>A NCBI36
NG_008077.1:g.5202G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.178G>T MANE Select ENSP00000251643.4:p.Ala60Ser
ENST00000647902.1:c.178G>T ENSP00000497770.1:p.Ala60Ser
ENST00000251643.4:c.178G>T ENSP00000251643.4:p.Ala60Ser
NM_000223.3:c.178G>T NP_000214.1:p.Ala60Ser
XR_934754.1:n.1500+16149C>A
XR_934754.2:n.2008+16149C>A
NM_000223.4:c.178G>T MANE Select NP_000214.1:p.Ala60Ser