Canonical Allele Identifier: CA590653187

Gene: SPOUT1

Genomic Alleles

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

Transcript Alleles

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