Canonical Allele Identifier: CA8549656

Gene: KRT23

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40930034G>T , CM000679.2:g.40930034G>T	GRCh38
NC_000017.10:g.39086286G>T , CM000679.1:g.39086286G>T	GRCh37
NC_000017.9:g.36339812G>T	NCBI36
NG_012287.1:g.12551C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015515.5:c.542C>A MANE Select	NP_056330.3:p.Thr181Asn
ENST00000209718.8:c.542C>A MANE Select	ENSP00000209718.3:p.Thr181Asn
NM_001282433.1:c.131C>A	NP_001269362.1:p.Thr44Asn
NM_001282433.2:c.131C>A	NP_001269362.1:p.Thr44Asn
NM_015515.4:c.542C>A	NP_056330.3:p.Thr181Asn
ENST00000209718.7:c.542C>A	ENSP00000209718.3:p.Thr181Asn
ENST00000436344.7:c.131C>A	ENSP00000414056.3:p.Thr44Asn
ENST00000462312.5:c.68+1339C>A	ENSP00000462335.1:n.68+1339C>A
ENST00000494691.5:c.68+1339C>A	ENSP00000464548.1:n.68+1339C>A
ENST00000582754.5:n.774C>A
ENST00000584517.1:c.329C>A	ENSP00000464051.1:p.Thr110Asn
XM_005257200.3:c.131C>A	XP_005257257.1:p.Thr44Asn
XM_005257200.5:c.131C>A	XP_005257257.1:p.Thr44Asn
XM_011524595.1:c.131C>A	XP_011522897.1:p.Thr44Asn
XM_011524595.2:c.131C>A	XP_011522897.1:p.Thr44Asn
XR_001752885.1:n.83+1352G>T
XR_001752886.1:n.83+1352G>T