Canonical Allele Identifier: CA3212580397

Gene: SPINT1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40853635A= , CM000677.2:g.40853635A=	GRCh38
NC_000015.9:g.41145833A= , CM000677.1:g.41145833A=	GRCh37
NC_000015.8:g.38933125A=	NCBI36
NG_029239.1:g.14588A=

Transcript Alleles

HGVS	Amino-acid Change
NM_003710.4:c.742+8A= MANE Select	NP_003701.1:n.742+8A=
ENST00000562057.6:c.742+8A= MANE Select	ENSP00000457076.1:n.742+8A=
NM_001032367.1:c.742+8A=	NP_001027539.1:n.742+8A=
NM_001032367.2:c.742+8A=	NP_001027539.1:n.742+8A=
NM_001386873.1:c.742+8A=	NP_001373802.1:n.742+8A=
NM_001386874.1:c.742+8A=	NP_001373803.1:n.742+8A=
NM_001386875.1:c.742+8A=	NP_001373804.1:n.742+8A=
NM_003710.3:c.742+8A=	NP_003701.1:n.742+8A=
NM_181642.2:c.742+8A=	NP_857593.1:n.742+8A=
NM_181642.3:c.742+8A=	NP_857593.1:n.742+8A=
ENST00000344051.8:c.742+8A=	ENSP00000342098.4:n.742+8A=
ENST00000562057.5:c.742+8A=	ENSP00000457076.1:n.742+8A=
ENST00000563656.5:c.742+8A=	ENSP00000457284.1:n.742+8A=
ENST00000564375.5:c.118+8A=	ENSP00000454315.1:n.118+8A=
ENST00000566928.5:c.195+8A=
ENST00000568580.5:c.622+8A=	ENSP00000458074.1:n.622+8A=
ENST00000568823.5:c.867+8A=
XM_006720657.1:c.742+8A=	XP_006720720.1:n.742+8A=
XM_011521957.1:c.742+8A=	XP_011520259.1:n.742+8A=
XM_011521957.2:c.742+8A=	XP_011520259.1:n.742+8A=
XM_011521958.1:c.742+8A=	XP_011520260.1:n.742+8A=
XM_011521958.2:c.742+8A=	XP_011520260.1:n.742+8A=