Canonical Allele Identifier: CA8549554

Gene: KRT23

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40928252T>C , CM000679.2:g.40928252T>C	GRCh38
NC_000017.10:g.39084504T>C , CM000679.1:g.39084504T>C	GRCh37
NC_000017.9:g.36338030T>C	NCBI36
NG_012287.1:g.14333A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000209718.8:c.907A>G MANE Select	ENSP00000209718.3:p.Thr303Ala
ENST00000209718.7:c.907A>G	ENSP00000209718.3:p.Thr303Ala
ENST00000436344.7:c.496A>G	ENSP00000414056.3:p.Thr166Ala
ENST00000462312.5:c.*225A>G	ENSP00000462335.1:n.*225A>G
ENST00000494691.5:c.*225A>G	ENSP00000464548.1:n.*225A>G
ENST00000582754.5:n.1139A>G
NM_001282433.1:c.496A>G	NP_001269362.1:p.Thr166Ala
NM_015515.4:c.907A>G	NP_056330.3:p.Thr303Ala
XM_005257200.3:c.496A>G	XP_005257257.1:p.Thr166Ala
XM_011524595.1:c.496A>G	XP_011522897.1:p.Thr166Ala
XM_005257200.5:c.496A>G	XP_005257257.1:p.Thr166Ala
XM_011524595.2:c.496A>G	XP_011522897.1:p.Thr166Ala
NM_001282433.2:c.496A>G	NP_001269362.1:p.Thr166Ala
NM_015515.5:c.907A>G MANE Select	NP_056330.3:p.Thr303Ala