Canonical Allele Identifier: CA13383532

Gene: MS4A4A MS4A4E

Linked Data

• dbSNP Id: rs670139
• gnomAD v2: 11-59971795-G-T
• gnomAD v3: 11-60204322-G-T
• gnomAD v4: 11-60204322-G-T
• MyVariant Identifiers: chr11:g.59971795G>T (hg19) ; chr11:g.60204322G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.60204322G>T , CM000673.2:g.60204322G>T	GRCh38
NC_000011.9:g.59971795G>T , CM000673.1:g.59971795G>T	GRCh37
NC_000011.8:g.59728371G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000649552.2:c.59+18151G>T (MS4A4A)	ENSP00000497952.2:n.59+18151G>T
ENST00000651255.1:c.659+568C>A (MS4A4E) MANE Select	ENSP00000499123.1:n.659+568C>A
ENST00000679385.1:c.-25+18151G>T (MS4A4A)	ENSP00000506313.1:n.-25+18151G>T
ENST00000679553.1:c.59+18151G>T (MS4A4A)	ENSP00000505712.1:n.59+18151G>T
ENST00000680301.1:c.59+18151G>T (MS4A4A)	ENSP00000506147.1:n.59+18151G>T
ENST00000680537.1:c.-176+18151G>T (MS4A4A)	ENSP00000506179.1:n.-176+18151G>T
ENST00000680560.1:c.59+18151G>T (MS4A4A)	ENSP00000505056.1:n.59+18151G>T
ENST00000680757.1:c.-105+18151G>T (MS4A4A)	ENSP00000505293.1:n.-105+18151G>T
ENST00000680935.1:c.-105+18151G>T (MS4A4A)	ENSP00000505050.1:n.-105+18151G>T
ENST00000681288.1:c.59+18151G>T (MS4A4A)	ENSP00000505714.1:n.59+18151G>T
ENST00000681406.1:c.59+18151G>T (MS4A4A)	ENSP00000505926.1:n.59+18151G>T
ENST00000532442.5:c.*139-2443C>A (MS4A4E)	ENSP00000435345.1:n.*139-2443C>A
XM_011545416.1:c.*102C>A (MS4A4E)	XP_011543718.1:n.*102C>A
XM_011545417.1:c.279-2443C>A (MS4A4E)	XP_011543719.1:n.279-2443C>A
XR_950143.1:n.1587+568C>A (MS4A4E)
XR_950144.1:n.1587+568C>A (MS4A4E)
NM_001351235.1:c.279-2443C>A (MS4A4E)	NP_001338164.1:n.279-2443C>A
XM_011545416.2:c.*102C>A (MS4A4E)	XP_011543718.1:n.*102C>A
XR_950143.2:n.1597+568C>A (MS4A4E)
XR_950144.2:n.1597+568C>A (MS4A4E)
NM_001351235.2:c.279-2443C>A (MS4A4E)	NP_001338164.1:n.279-2443C>A
NM_001393391.1:c.659+568C>A (MS4A4E) MANE Select	NP_001380320.1:n.659+568C>A