Canonical Allele Identifier: CA386013826
Gene: KERA HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.91449492T>G (hg19) chr12:g.91055715T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91055715T>G , CM000674.2:g.91055715T>G GRCh38
NC_000012.11:g.91449492T>G , CM000674.1:g.91449492T>G GRCh37
NC_000012.10:g.89973623T>G NCBI36
NG_021223.1:g.7640A>C , LRG_538:g.7640A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000266719.4:c.567A>C MANE Select ENSP00000266719.3:p.Lys189Asn
ENST00000266719.3:c.567A>C ENSP00000266719.3:p.Lys189Asn
NM_007035.3:c.567A>C , LRG_538t1:c.567A>C NP_008966.1:p.Lys189Asn
XM_011537781.1:c.567A>C XP_011536083.1:p.Lys189Asn
NM_007035.4:c.567A>C MANE Select NP_008966.1:p.Lys189Asn
Search 100 bp 5'
Search 100 bp 3'