Canonical Allele Identifier: CA2362515418

Gene: SRC

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.37358250G= , CM000682.2:g.37358250G=	GRCh38
NC_000020.10:g.35986653G= , CM000682.1:g.35986653G=	GRCh37
NC_000020.9:g.35420067G=	NCBI36
NG_023033.1:g.18566G= , LRG_1018:g.18566G=

Transcript Alleles

HGVS	Amino-acid Change
NM_198291.3:c.-246-6954G= MANE Select	NP_938033.1:n.-246-6954G=
ENST00000373578.7:c.-246-6954G= MANE Select	ENSP00000362680.2:n.-246-6954G=
NM_005417.4:c.-246-6954G=	NP_005408.1:n.-246-6954G=
NM_005417.5:c.-246-6954G=	NP_005408.1:n.-246-6954G=
NM_198291.2:c.-246-6954G= , LRG_1018t1:c.-246-6954G=	NP_938033.1:n.-246-6954G=
ENST00000373578.6:c.-246-6954G=	ENSP00000362680.2:n.-246-6954G=
ENST00000497734.5:n.204-6954G=
ENST00000692112.1:c.-246-6954G=	ENSP00000508666.1:n.-246-6954G=
ENST00000692423.1:c.-364-6954G=	ENSP00000509325.1:n.-364-6954G=
ENST00000693012.1:c.-246-6954G=	ENSP00000510370.1:n.-246-6954G=
XM_011529013.1:c.-246-6954G=	XP_011527315.1:n.-246-6954G=
XM_011529013.2:c.-246-6954G=	XP_011527315.1:n.-246-6954G=
XM_017028024.1:c.-246-6954G=	XP_016883513.1:n.-246-6954G=
XM_017028025.1:c.-246-6954G=	XP_016883514.1:n.-246-6954G=
XM_017028026.1:c.-246-6954G=	XP_016883515.1:n.-246-6954G=