Canonical Allele Identifier: CA1814596288

Gene: MAL2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.119212466C= , CM000670.2:g.119212466C=	GRCh38
NC_000008.10:g.120224706C= , CM000670.1:g.120224706C=	GRCh37
NC_000008.9:g.120293887C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000614891.5:c.132+3862C= MANE Select	ENSP00000479708.1:n.132+3862C=
ENST00000522112.6:c.-72-9121C=	ENSP00000483044.1:n.-72-9121C=
ENST00000531508.1:c.-73+3266C=	ENSP00000484544.1:n.-73+3266C=
ENST00000534619.5:c.-73+4373C=	ENSP00000482729.1:n.-73+4373C=
ENST00000614891.4:c.132+3862C=	ENSP00000479708.1:n.132+3862C=
NM_052886.2:c.132+3862C=	NP_443118.1:n.132+3862C=
XM_011516807.1:c.132+3862C=	XP_011515109.1:n.132+3862C=
XM_011516807.2:c.132+3862C=	XP_011515109.1:n.132+3862C=
NM_052886.3:c.132+3862C= MANE Select	NP_443118.1:n.132+3862C=