Canonical Allele Identifier: CA1976874658

Gene: MS4A1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.60464852A>T , CM000673.2:g.60464852A>T	GRCh38
NC_000011.9:g.60232325A>T , CM000673.1:g.60232325A>T	GRCh37
NC_000011.8:g.59988901A>T	NCBI36
NG_023388.1:g.14044A>T , LRG_140:g.14044A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345732.9:c.336+508A>T MANE Select	ENSP00000314620.7:n.336+508A>T
ENST00000533306.6:c.288+508A>T	ENSP00000437002.2:n.288+508A>T
ENST00000534668.6:c.336+508A>T	ENSP00000433277.1:n.336+508A>T
ENST00000674194.1:c.336+508A>T	ENSP00000501369.1:n.336+508A>T
ENST00000345732.8:c.336+508A>T	ENSP00000314620.7:n.336+508A>T
ENST00000389939.2:c.336+508A>T	ENSP00000374589.2:n.336+508A>T
ENST00000528313.1:c.112-2146A>T	ENSP00000432270.1:n.112-2146A>T
ENST00000532073.5:c.336+508A>T	ENSP00000433519.1:n.336+508A>T
ENST00000533306.5:c.345+508A>T	ENSP00000437002.1:n.345+508A>T
ENST00000534668.5:c.336+508A>T	ENSP00000433277.1:n.336+508A>T
NM_021950.3:c.336+508A>T	NP_068769.2:n.336+508A>T
NM_152866.2:c.336+508A>T , LRG_140t1:c.336+508A>T	NP_690605.1:n.336+508A>T
NM_152866.3:c.336+508A>T MANE Select	NP_690605.1:n.336+508A>T
NM_152867.2:c.336+508A>T	NP_690606.1:n.336+508A>T
NM_021950.4:c.336+508A>T	NP_068769.2:n.336+508A>T