Canonical Allele Identifier: CA1976737985

Gene: MS4A6A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.60173126T= , CM000673.2:g.60173126T=	GRCh38
NC_000011.9:g.59940599T= , CM000673.1:g.59940599T=	GRCh37
NC_000011.8:g.59697175T=	NCBI36
NG_033978.1:g.16541A=

Transcript Alleles

HGVS	Amino-acid Change
NM_022349.4:c.553A= MANE Select	NP_071744.2:p.Thr185=
ENST00000528851.6:c.553A= MANE Select	ENSP00000431901.1:p.Thr185=
NM_001247999.1:c.637A=	NP_001234928.1:p.Thr213=
NM_001247999.2:c.637A=	NP_001234928.1:p.Thr213=
NM_001330275.1:c.637A=	NP_001317204.1:p.Thr213=
NM_022349.3:c.553A=	NP_071744.2:p.Thr185=
NM_152851.2:c.449A=	NP_690590.1:p.Asn150=
NM_152852.2:c.553A=	NP_690591.1:p.Thr185=
NM_152852.3:c.553A=	NP_690591.1:p.Thr185=
ENST00000412309.6:c.637A=	ENSP00000403212.2:p.Thr213=
ENST00000420732.6:c.449A=	ENSP00000392921.2:p.Asn150=
ENST00000426738.6:c.637A=	ENSP00000392770.3:p.Thr213=
ENST00000527254.5:c.*225A=	ENSP00000435630.1:n.*225A=
ENST00000528851.5:c.553A=	ENSP00000431901.1:p.Thr185=
ENST00000529054.5:c.637A=	ENSP00000435844.1:p.Thr213=
ENST00000530839.5:c.553A=	ENSP00000436979.1:p.Thr185=
ENST00000531914.5:n.308A=
ENST00000533023.5:c.257A=	ENSP00000436172.1:p.Asn86=
ENST00000533989.5:c.253A=
XM_005274177.1:c.637A=	XP_005274234.1:p.Thr213=
XM_005274177.3:c.637A=	XP_005274234.1:p.Thr213=
XM_005274178.1:c.637A=	XP_005274235.1:p.Thr213=
XM_006718658.1:c.637A=	XP_006718721.1:p.Thr213=
XM_006718659.1:c.637A=	XP_006718722.1:p.Thr213=
XM_006718660.1:c.502A=	XP_006718723.1:p.Thr168=
XM_006718660.2:c.502A=	XP_006718723.1:p.Thr168=
XM_006718661.1:c.502A=	XP_006718724.1:p.Thr168=
XM_006718661.2:c.502A=	XP_006718724.1:p.Thr168=
XM_006718662.1:c.418A=	XP_006718725.1:p.Thr140=
XM_006718663.1:c.418A=	XP_006718726.1:p.Thr140=
XM_011545208.1:c.553A=	XP_011543510.1:p.Thr185=
XM_024448652.1:c.637A=	XP_024304420.1:p.Thr213=
XM_024448653.1:c.553A=	XP_024304421.1:p.Thr185=
XM_024448654.1:c.418A=	XP_024304422.1:p.Thr140=
XM_024448655.1:c.418A=	XP_024304423.1:p.Thr140=