Canonical Allele Identifier: CA481306637
Gene: KERA HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.91449449G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91055672G>A , CM000674.2:g.91055672G>A GRCh38
NC_000012.11:g.91449449G>A , CM000674.1:g.91449449G>A GRCh37
NC_000012.10:g.89973580G>A NCBI36
NG_021223.1:g.7683C>T , LRG_538:g.7683C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000266719.4:c.610C>T MANE Select ENSP00000266719.3:p.Leu204=
ENST00000266719.3:c.610C>T ENSP00000266719.3:p.Leu204=
NM_007035.3:c.610C>T , LRG_538t1:c.610C>T NP_008966.1:p.Leu204=
XM_011537781.1:c.610C>T XP_011536083.1:p.Leu204=
NM_007035.4:c.610C>T MANE Select NP_008966.1:p.Leu204=