Canonical Allele Identifier: CA2576594975

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7122825G>A , CM000681.2:g.7122825G>A	GRCh38
NC_000019.9:g.7122836G>A , CM000681.1:g.7122836G>A	GRCh37
NC_000019.8:g.7073836G>A	NCBI36
NG_008852.2:g.176176C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3370-52C>T MANE Select	ENSP00000303830.4:n.3370-52C>T
ENST00000302850.9:c.3370-52C>T	ENSP00000303830.4:n.3370-52C>T
ENST00000341500.9:c.3334-52C>T	ENSP00000342838.4:n.3334-52C>T
ENST00000593970.1:n.216-52C>T
ENST00000601099.1:n.281-52C>T
NM_000208.2:c.3370-52C>T	NP_000199.2:n.3370-52C>T
NM_000208.3:c.3370-52C>T	NP_000199.2:n.3370-52C>T
NM_001079817.1:c.3334-52C>T	NP_001073285.1:n.3334-52C>T
NM_001079817.2:c.3334-52C>T	NP_001073285.1:n.3334-52C>T
XM_011527988.1:c.3445-52C>T	XP_011526290.1:n.3445-52C>T
XM_011527989.1:c.3409-52C>T	XP_011526291.1:n.3409-52C>T
XM_011527988.2:c.3367-52C>T	XP_011526290.2:n.3367-52C>T
XM_011527989.3:c.3331-52C>T	XP_011526291.2:n.3331-52C>T
NM_000208.4:c.3370-52C>T MANE Select	NP_000199.2:n.3370-52C>T
NM_001079817.3:c.3334-52C>T	NP_001073285.1:n.3334-52C>T