Canonical Allele Identifier: CA386014405
Gene: KERA HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.91449756A>T (hg19) chr12:g.91055979A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91055979A>T , CM000674.2:g.91055979A>T GRCh38
NC_000012.11:g.91449756A>T , CM000674.1:g.91449756A>T GRCh37
NC_000012.10:g.89973887A>T NCBI36
NG_021223.1:g.7376T>A , LRG_538:g.7376T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000266719.4:c.303T>A MANE Select ENSP00000266719.3:p.Asn101Lys
ENST00000266719.3:c.303T>A ENSP00000266719.3:p.Asn101Lys
NM_007035.3:c.303T>A , LRG_538t1:c.303T>A NP_008966.1:p.Asn101Lys
XM_011537781.1:c.303T>A XP_011536083.1:p.Asn101Lys
NM_007035.4:c.303T>A MANE Select NP_008966.1:p.Asn101Lys
Search 100 bp 5'
Search 100 bp 3'