Canonical Allele Identifier: CA481306656
Gene: KERA HGNC NCBI

Linked Data

gnomAD v4: 12-91055562-G-A
COSMIC: COSM3466354
MyVariant Identifiers: chr12:g.91449339G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91055562G>A , CM000674.2:g.91055562G>A GRCh38
NC_000012.11:g.91449339G>A , CM000674.1:g.91449339G>A GRCh37
NC_000012.10:g.89973470G>A NCBI36
NG_021223.1:g.7793C>T , LRG_538:g.7793C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000266719.4:c.720C>T MANE Select ENSP00000266719.3:p.Ala240=
ENST00000266719.3:c.720C>T ENSP00000266719.3:p.Ala240=
NM_007035.3:c.720C>T , LRG_538t1:c.720C>T NP_008966.1:p.Ala240=
XM_011537781.1:c.720C>T XP_011536083.1:p.Ala240=
NM_007035.4:c.720C>T MANE Select NP_008966.1:p.Ala240=
Search 100 bp 5'
Search 100 bp 3'