Canonical Allele Identifier: CA1880482623

Gene: SPOUT1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.128824961G= , CM000671.2:g.128824961G=	GRCh38
NC_000009.11:g.131587240G= , CM000671.1:g.131587240G=	GRCh37
NC_000009.10:g.130627061G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_016390.4:c.712+16C= MANE Select	NP_057474.2:n.712+16C=
ENST00000361256.10:c.712+16C= MANE Select	ENSP00000354812.5:n.712+16C=
NM_016390.3:c.712+16C=	NP_057474.2:n.712+16C=
ENST00000361256.9:c.712+16C=	ENSP00000354812.5:n.712+16C=
ENST00000480366.1:n.275+16C=
ENST00000622809.1:c.709+16C=	ENSP00000481659.1:n.709+16C=
ENST00000651925.1:c.*1751+16C=	ENSP00000498386.1:n.*1751+16C=
XM_005252045.3:c.712+16C=	XP_005252102.2:n.712+16C=
XM_011518773.1:c.712+16C=	XP_011517075.1:n.712+16C=
XM_011518774.1:c.712+16C=	XP_011517076.1:n.712+16C=
XM_011518775.1:c.712+16C=	XP_011517077.1:n.712+16C=
XM_017014804.1:c.958+16C=	XP_016870293.1:n.958+16C=