Canonical Allele Identifier: CA1907214770

Gene: MSMB

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.46036353G= , CM000672.2:g.46036353G=	GRCh38
NC_000010.10:g.51559469C= , CM000672.1:g.51559469C=	GRCh37
NC_000010.9:g.51229475C=	NCBI36
NG_011551.1:g.14917C=

Transcript Alleles

HGVS	Amino-acid Change
NM_002443.4:c.215+2613C= MANE Select	NP_002434.1:n.215+2613C=
ENST00000582163.3:c.215+2613C= MANE Select	ENSP00000463092.1:n.215+2613C=
NM_002443.3:c.215+2613C=	NP_002434.1:n.215+2613C=
NM_138634.2:c.110-2802C=	NP_619540.1:n.110-2802C=
NM_138634.3:c.110-2802C=	NP_619540.1:n.110-2802C=
ENST00000581478.5:c.110-2802C=	ENSP00000462641.1:n.110-2802C=
ENST00000582163.2:c.215+2613C=	ENSP00000463092.1:n.215+2613C=
ENST00000663171.1:c.215+2613C=	ENSP00000499419.1:n.215+2613C=
XR_945923.1:n.1284G=
XR_945923.3:n.1284G=