Canonical Allele Identifier: CA399388928

Gene: KRT12

Linked Data

• MyVariant Identifiers: chr17:g.39023185T>A (hg19) ; chr17:g.40866933T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40866933T>A , CM000679.2:g.40866933T>A	GRCh38
NC_000017.10:g.39023185T>A , CM000679.1:g.39023185T>A	GRCh37
NC_000017.9:g.36276711T>A	NCBI36
NG_008077.1:g.5278A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251643.5:c.254A>T MANE Select	ENSP00000251643.4:p.Tyr85Phe
ENST00000647902.1:c.211+43A>T	ENSP00000497770.1:n.211+43A>T
ENST00000251643.4:c.254A>T	ENSP00000251643.4:p.Tyr85Phe
NM_000223.3:c.254A>T	NP_000214.1:p.Tyr85Phe
XR_934754.1:n.1500+16073T>A
XR_934754.2:n.2008+16073T>A
NM_000223.4:c.254A>T MANE Select	NP_000214.1:p.Tyr85Phe