Canonical Allele Identifier: CA1814596326

Gene: MAL2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.119212521A= , CM000670.2:g.119212521A=	GRCh38
NC_000008.10:g.120224761A= , CM000670.1:g.120224761A=	GRCh37
NC_000008.9:g.120293942A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000614891.5:c.132+3917A= MANE Select	ENSP00000479708.1:n.132+3917A=
ENST00000522112.6:c.-72-9066A=	ENSP00000483044.1:n.-72-9066A=
ENST00000531508.1:c.-73+3321A=	ENSP00000484544.1:n.-73+3321A=
ENST00000534619.5:c.-73+4428A=	ENSP00000482729.1:n.-73+4428A=
ENST00000614891.4:c.132+3917A=	ENSP00000479708.1:n.132+3917A=
NM_052886.2:c.132+3917A=	NP_443118.1:n.132+3917A=
XM_011516807.1:c.132+3917A=	XP_011515109.1:n.132+3917A=
XM_011516807.2:c.132+3917A=	XP_011515109.1:n.132+3917A=
NM_052886.3:c.132+3917A= MANE Select	NP_443118.1:n.132+3917A=