Canonical Allele Identifier: CA399389580
Gene: KRT12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.39023350G>T (hg19) chr17:g.40867098G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.40867098G>T , CM000679.2:g.40867098G>T GRCh38
NC_000017.10:g.39023350G>T , CM000679.1:g.39023350G>T GRCh37
NC_000017.9:g.36276876G>T NCBI36
NG_008077.1:g.5113C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000251643.5:c.89C>A MANE Select ENSP00000251643.4:p.Pro30His
ENST00000647902.1:c.89C>A ENSP00000497770.1:p.Pro30His
ENST00000251643.4:c.89C>A ENSP00000251643.4:p.Pro30His
NM_000223.3:c.89C>A NP_000214.1:p.Pro30His
XR_934754.1:n.1500+16238G>T
XR_934754.2:n.2008+16238G>T
NM_000223.4:c.89C>A MANE Select NP_000214.1:p.Pro30His
Search 100 bp 5'
Search 100 bp 3'