Canonical Allele Identifier: CA500187325
Gene: KRT12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39023220G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40866968G>T , CM000679.2:g.40866968G>T GRCh38
NC_000017.10:g.39023220G>T , CM000679.1:g.39023220G>T GRCh37
NC_000017.9:g.36276746G>T NCBI36
NG_008077.1:g.5243C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.219C>A MANE Select ENSP00000251643.4:p.Ser73=
ENST00000647902.1:c.211+8C>A ENSP00000497770.1:n.211+8C>A
ENST00000251643.4:c.219C>A ENSP00000251643.4:p.Ser73=
NM_000223.3:c.219C>A NP_000214.1:p.Ser73=
XR_934754.1:n.1500+16108G>T
XR_934754.2:n.2008+16108G>T
NM_000223.4:c.219C>A MANE Select NP_000214.1:p.Ser73=