Canonical Allele Identifier: CA386013551

Gene: KERA

Linked Data

• dbSNP Id: rs1468891558
• MyVariant Identifiers: chr12:g.91449368T>A (hg19) ; chr12:g.91055591T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91055591T>A , CM000674.2:g.91055591T>A	GRCh38
NC_000012.11:g.91449368T>A , CM000674.1:g.91449368T>A	GRCh37
NC_000012.10:g.89973499T>A	NCBI36
NG_021223.1:g.7764A>T , LRG_538:g.7764A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266719.4:c.691A>T MANE Select	ENSP00000266719.3:p.Asn231Tyr
ENST00000266719.3:c.691A>T	ENSP00000266719.3:p.Asn231Tyr
NM_007035.3:c.691A>T , LRG_538t1:c.691A>T	NP_008966.1:p.Asn231Tyr
XM_011537781.1:c.691A>T	XP_011536083.1:p.Asn231Tyr
NM_007035.4:c.691A>T MANE Select	NP_008966.1:p.Asn231Tyr